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1 December 2007

Volume 196, Number 11
The Journal of Infectious Diseases 2007;196:1698–1706
0022-1899/2007/19611-0019$15.00
DOI: 10.1086/522147
MAJOR ARTICLE

CD14 C(−159)T Polymorphism Is a Risk Factor for Development of Pulmonary Tuberculosis

Adrian G. Rosas‐Taraco,1

Agnès Revol,1

Mario C. Salinas‐Carmona,1

Adrian Rendon,2

Guillermo Caballero‐Olin,3 and

Alma Y. Arce‐Mendoza1

1Departamento Inmunologia, Facultad de Medicina, 2CIPTIR (Centro de Investigacion, Prevencion y Tratamiento de Infecciones Respiratorias), Hospital Universitario, UANL, and 3Instituto Mexicano del Seguro Social, Monterrey, Nuevo León, México

Background.Neither the expression of CD14 and Toll‐like receptor 4 (TLR4) on monocytes’ surface nor the mutations CD14 −159TT and TLR4 Asp299Gly have yet been evaluated as risk factors for development of pulmonary tuberculosis (TB) in the Mexican population.

Methods.Level of membrane CD14 (mCD14) and membrane TLR4 (mTLR4) were determined by flow cytometry, in 104 patients with pulmonary TB (before and after treatment), 67 household contacts, and 114 healthy control subjects. Genotype/allele frequencies in CD14 ‐159 and TLR4 Asp299Gly were obtained by polymerase chain reaction–restriction‐fragment length polymorphism. Levels of soluble CD14 (sCD14) in sera were quantified by ELISA.

Results.Higher levels of mCD14/sCD14 and mTLR4 were observed in the patients and the household contacts than in the control subjects ( ) and decreased in the patients after the infection was resolved. The frequency of the CD14 −159TT genotype was higher in the patients than in the control subjects (35.6% vs. 12.3%, respectively). Patients who were homozygous for allele T of the CD14 promoter gene had a significantly higher risk for development of pulmonary TB, with an odds ratio of 2.267 (95% confidence interval, 1.5%–3.3%). Levels of sCD14 or mCD14 were not associated with the CD14 −159TT genotype ( ).

Conclusions.No association between TLR4 Asp299Gly and pulmonary TB was found. CD14 −159TT is a risk factor for development of pulmonary TB, whereas mCD14/sCD14 and mTLR4 are possible biomarkers for the prognosis for TB disease.

Clinical Trial Protocol ID: SA1168‐05.

Received 30 January 2007; accepted 22 June 2007; electronically published 25 October 2007.

Reprints or correspondence: Dr. Alma Yolanda Arce‐Mandoza, Departamento Inmunología, Facultad Medicina, Universidad Autónoma de Nuevo León, Gonzalitos 235 Norte, Mitras Centro, Monterrey, Nuevo León, México 64460 ().

Global Theme Issue: Poverty and Human Development

Cited by

S Mahasirimongkol, H Yanai, N Nishida, C Ridruechai, I Matsushita, J Ohashi, S Summanapan, N Yamada, S Moolphate, C Chuchotaworn, A Chaiprasert, W Manosuthi, P Kantipong, S Kanitwittaya, T Sura, S Khusmith, K Tokunaga, P Sawanpanyalert, N Keicho. (2008) Genome-wide SNP-based linkage analysis of tuberculosis in Thais. Genes and Immunity
Online publication date: 9-Nov-2008.
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  • Potential conflicts of interest: none reported.

    Financial support: Programa de Apoyo a la Investigaci|$$|Aaon Cient|$$|Aaifica y Tecnol|$$|Aaogica (PAICYT), Universidad Autonoma de Nuevo Leon (grant SA1168‐05 to A.Y.A.-M.).

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